Clinical Research Coordinator
AI summary
NexGen Research Ltd is hiring a detail-oriented Clinical Research Coordinator based in Enugu, Nigeria to support global clinical trial operations remotely. The role involves regulatory document management, data entry, study tracking, and quality assurance, with a competitive salary of NGN 250,000–400,000. Candidates need a bachelor’s degree in a health/life sciences field, strong English and computer skills, and availability during U.S. business hours.
- Remote role supporting global clinical trials from Enugu
- Salary range NGN 250,000 – 400,000
- Entry level with 1 year experience required
- Must be available during U.S. Eastern business hours
- Comprehensive clinical research training and mentorship provided
AI job guide
Use this guide to check salary signals, requirements, documents, application steps and safety before you apply.
AI salary guide
Source salary availableThe source lists NGN 250,000 - 400,000. Confirm the final pay, benefits, contract terms and allowances directly with the employer before accepting an offer.
Can you qualify for this role?
- Required1+ years of relevant experienceThe job post includes a minimum experience signal.
- RequiredEducation or certification mentioned in the postThe captured text mentions education, a diploma, certificate, or licence.
- PreferredPractical evidence in internship, no_experience, Clinical ResearchThe tags and summary point to skills connected with this role.
- RequiredAvailability to work in EnuguThe vacancy is associated with this location.
- UnclearComfort with the Full Time contract termsConfirm hours, duration, probation and benefits at the original source.
Documents to prepare
- Likely requiredUpdated CV
- Role specificCover letter or short employer message
- OptionalProfessional references
- Role specificAcademic or professional certificates
- VerifyID or passport only after verifying the employer
Application tips for this job
- Place your strongest Clinical Research Coordinator evidence in the first half of your CV.
- In your cover letter or employer message, connect your experience to NexGen Research Ltd and the role in Enugu.
- Add concrete examples related to internship, no_experience, Clinical Research, ideally with measurable outcomes or clear responsibilities.
- Follow the instructions from Jobberman Nigeria; avoid sending documents to unofficial contacts or copied links.
- Confirm the deadline, interview location and employer contact before sharing personal documents.
Source and safety check
- Jobberman Nigeria
- Original source link available
- Application method is clear
- Deadline not specified
- No major risk signal was detected in the captured text.
Never pay for interviews, shortlisting, medical checks, uniforms, or job placement. Confirm every application at the original source before sharing personal documents. Report suspicious listing.
Interview preparation
- What experience makes you a strong fit for this Clinical Research Coordinator role in internship, no_experience?
- How have you handled responsibilities similar to those in this job post?
- Are you available to work in Enugu under the listed contract or schedule?
- Prepare examples with clear responsibilities, tools used and measurable outcomes.
- Review the source and research NexGen Research Ltd before the interview.
Ask what the first priorities will be in the role and how success will be measured.
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Original source description
Clinical Research Coordinator NexGen Research Ltd Research, Teaching & Training Yesterday Easy apply New Enugu Full Time Healthcare NGN 250,000 - 400,000 Share link Share on WhatsApp Share on LinkedIn Share on Facebook Share on Twitter Share via SMS Job summary NexGen Research is seeking a detail-oriented Clinical Research Coordinator to support global clinical trial operations remotely. Responsibilities: include regulatory document management, data entry, study tracking, and quality assurance activities. Strong computer skills, excellent English communication, and availability during U.S. Eastern time. Min Qualification: Degree Experience: Level: Entry level Experience: Length: 1 year Language Requirement: English Working Hours: Full Time - 8 to 5 Applicant Location: Enugu, Nigeria Job descriptions & requirements: Responsibilities: Assist with clinical trial regulatory document management Prepare and maintain electronic regulatory binders Enter and review study data in Electronic Data Capture (EDC) systems Track study documentation and investigator training records Support subject recruitment and pre-screening activities Assist with adverse event and protocol deviation documentation Review medical records and source documents for completeness Prepare reports, logs, trackers, and study-related correspondence Schedule investigator meetings and training sessions Support quality assurance and compliance activities Coordinate with investigators, sponsors, and CROs globally Requirements: Bachelor's degree or higher in: Medicine, Nursing, Pharmacy, Medical Laboratory Science, Public Health, Biological Sciences, and Life Sciences or related field Excellent written and spoken English Strong computer skills and proficiency with Microsoft Office Reliable internet connection and personal computer Close attention to detail and ability to meet deadlines Ability to work during U.S. business hours Preferred Qualifications: Prior clinical research experience: GCP certification Experience: with EDC systems Experience: with regulatory documentation Healthcare or medical records experience: Benefits: Comprehensive clinical research training Exposure to global clinical trial operations Career development opportunities Mentorship from experienced investigators and research professionals Competitive compensation Long-term growth potential within a rapidly expanding research organization Log In and Apply Important safety tips Do not make any payment without confirming with the Jobberman Customer Support Team. If you think this advert is not genuine, please report it via the Report Job link below. Report Job